Data Foundry

Medical device recalls 2024

Azurion 5 with a Certeray generator-To perform image guidance in… — Class II medical device recall Z-1177-2024

Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2024-02-28, distributed nationwide. Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR

Recall numberZ-1177-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, N/A, Netherlands
Recall initiated2024-02-06
Classified2024-02-22
Reported by FDA2024-02-28
DistributedNationwide (US)
Countries outside the USAT, BR, CH, CN, CO, CZ, DE, DZ, EC, ES, FR, GB, HR, HU, ID, IL, IN, IQ, IT, JP, KR, KW, LT, MA, MY, NL, NO, OM, PA, PL, PT, QA, RO, SA, SE, TN, TR, TW, UA
Quantity27 units
Reason classesdevice malfunction
UPC / GTIN / UDI-DI00884838086777, 00884838099227, 00884838099234
Serial numbers139, 141, 147, 154, 161, 163, 165, 167, 168, 171, 174, 176, 178, 193, 194, 197, 200, 202, 208, 228
Model numbers722227, 722228

Product

Azurion 5 with a Certeray generator-To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722227 (2) 722228

Reason for recall

Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1177-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.